ライフサイエンスコーパス: Thermoplasma

1 r weight TrxR from the thermophilic archaeon Thermoplasma acidophilum ( taTrxR) that is characterized

2 Citrate synthases from Thermoplasma acidophilum (optimal growth at 55 degrees C

3 by a serine in proteasomes from the archaeon Thermoplasma acidophilum (T1S mutant) does not alter the

4 ture of the N-terminal MCM from the archaeon Thermoplasma acidophilum (tapMCM).

5 anothermobacter thermautotrophicus (MTH) and Thermoplasma acidophilum (THA), and the His-tagged recom

6 itrate synthase from a moderate thermophile, Thermoplasma acidophilum (TpCS), are compared with those

7 Valosin-containing protein-like ATPase of Thermoplasma acidophilum (VAT), the archaeal homolog of

8 We report here the structure of the 700 kDa Thermoplasma acidophilum 20S proteasome (T20S), determin

9 d structural simplicity, the archaebacterium Thermoplasma Acidophilum 20S proteasome was selected for

10 mately 700-kDa protein with D7 symmetry, the Thermoplasma acidophilum 20S proteasome, showing clear s

11 ned a 3.2 A resolution reconstruction of the Thermoplasma acidophilum 20S proteasome.

12 the well characterized 20 S proteasomes from Thermoplasma acidophilum and ATP, this complex stimulate

13 orming subunits E and H of the A-ATPase from Thermoplasma acidophilum and demonstrated that the two p

14 Using proteasomes from Thermoplasma acidophilum and four unfolded polypeptides

15 vered in most Archaea (with the exception of Thermoplasma acidophilum and Halobacterium NRC-1) and so

16 e alpha-subunits of the CP from the archaeon Thermoplasma acidophilum are arranged such that, on aver

17 from the thermophilic heterotrophic archaea Thermoplasma acidophilum at 1.6 A resolution, in complex

18 The BBS6 protein has similarity to a Thermoplasma acidophilum chaperonin, whereas BBS2 and BB

19 the condensation half-reaction performed by Thermoplasma acidophilum citrate synthase (TpCS) with th

20 ermus ruber library with probes made against Thermoplasma acidophilum DNA yielded a number of clones

21 tion is based on the oxidation of glucose by Thermoplasma acidophilum glucose dehydrogenase with the

22 gh the structure of the 20 S proteasome from Thermoplasma acidophilum has been elucidated, its enzyma

23 NA binding by the archaeal XPD helicase from Thermoplasma acidophilum has been investigated using a c

24 VAT, the Thermoplasma acidophilum homologue of eukaryotic CDC48/p

25 we find that Cdc48 and 20S from the archaeon Thermoplasma acidophilum interact to form a functional p

26 that FANCM and its archaeal homolog Hef from Thermoplasma acidophilum interact with proliferating cel

27 The thermosome from Thermoplasma acidophilum is a type II chaperonin compose

28 ction catalyzed by the citrate synthase from Thermoplasma acidophilum is accompanied by changes in tr

29 hat seen in Methanococcus and Halobacterium, Thermoplasma acidophilum lacks the RNase P subunits.

30 Two x-ray structures of the Thermoplasma acidophilum LplA structure have been report

31 e encoding a zinc-containing ferredoxin from Thermoplasma acidophilum strain HO-62 was cloned and seq

32 a putative lipoate protein ligase (LplA) of Thermoplasma acidophilum was cloned and expressed in Esc

33 The crystallographic structure of RbkR from Thermoplasma acidophilum was determined in complex with

34 eta-thermosome, the class II chaperonin from Thermoplasma acidophilum, by introducing a (His)6-tag wi

35 Indeed, Thermoplasma acidophilum, which lacks PAN, encodes one C

36 ing on the 20S proteasome core particle from Thermoplasma acidophilum.

37 xR (Ta0984) and a putative Trx (Ta0866) from Thermoplasma acidophilum.

38 -ATPase from the thermoacidophilic Archaeon, Thermoplasma acidophilum.

39 in the thermosome, a type II chaperonin from Thermoplasma acidophilum.

40 TA0175 as phosphoglycolate phosphatase from Thermoplasma acidophilum.

41 f a prokaryotic chaperonin in the thermosome Thermoplasma acidophilum.

42 yrococcus spp., Sulfolobus solfataricus, and Thermoplasma acidophilum.

43 ed by sulfidogenic wall-less archaebacteria (thermoplasmas) after aerotolerant cytoplasmic-tubule-con

44 are under way, including two halophiles, two Thermoplasma, and a methanogen.

45 cterium, a thermoacidophil resembling extant Thermoplasma, generated hydrogen sulfide to protect the

46 ell fusion between members of Archaea (e.g., Thermoplasma-like organisms) and of Eubacteria (e.g., Sp

47 Modification of Thermoplasma proteasomes demonstrates the requirement fo

48 Thermoplasma proteasomes, which contain one type of acti

49 potassium channel cloned from the prokaryote Thermoplasma volcanium.

50 ethanosarcina, Methanococcus, Archaeoglobus, Thermoplasma), with multiple genes in some species.

51 pared to those regions in the proteasomes of Thermoplasma, yeast, and mammalian cells, suggesting tha